Related MeSH Hierarchy (8)
Diseases [C] » Neoplasms [C04] » Neoplasms by Site » Nervous System Neoplasms » Central Nervous System Neoplasms » Brain Neoplasms » Supratentorial Neoplasms » Hypothalamic Neoplasms » Pallister-Hall Syndrome
Diseases [C] » Musculoskeletal Diseases [C05] » Musculoskeletal Abnormalities » Limb Deformities, Congenital » Polydactyly » Pallister-Hall Syndrome
Diseases [C] » Nervous System Diseases [C10] » Central Nervous System Diseases » Brain Diseases » Brain Neoplasms » Supratentorial Neoplasms » Hypothalamic Neoplasms » Pallister-Hall Syndrome
Diseases [C] » Nervous System Diseases [C10] » Central Nervous System Diseases » Brain Diseases » Hypothalamic Diseases » Hypothalamic Neoplasms » Pallister-Hall Syndrome
Diseases [C] » Nervous System Diseases [C10] » Nervous System Neoplasms » Central Nervous System Neoplasms » Brain Neoplasms » Supratentorial Neoplasms » Hypothalamic Neoplasms » Pallister-Hall Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Abnormalities, Multiple » Pallister-Hall Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Musculoskeletal Abnormalities » Limb Deformities, Congenital » Polydactyly » Pallister-Hall Syndrome
Description
A pleiotropic disorder of human development that comprises hypothalamic HAMARTOMA; central and postaxial POLYDACTYLY; bifid EPIGLOTTIS; ANAL ATRESIA; and renal and other abnormalities. This disorder is associated with FRAMESHIFT MUTATIONS in the GLI3 gene which encodes the GLI3 protein, a KRUPPEL-LIKE TRANSCRIPTION FACTORS family member. MeSH
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